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Br J Cancer. 1990 Nov;62(5):830-3. doi: 10.1038/bjc.1990.387.
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本文引用的文献

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VP 16-213 and cytosine-arabinoside combination chemotherapy for refractory acute lymphoblastic leukemia in adults.VP 16 - 213与阿糖胞苷联合化疗治疗成人难治性急性淋巴细胞白血病
Eur J Cancer Clin Oncol. 1984 Dec;20(12):1471-5. doi: 10.1016/0277-5379(84)90138-x.
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The place of bone-marrow transplantation in acute myelogenous leukaemia.骨髓移植在急性髓性白血病中的地位
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Cyclosporin A to prevent graft-versus-host disease in man after allogeneic bone-marrow transplantation.环孢素A预防异基因骨髓移植后人类的移植物抗宿主病。
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Comparison of three remission induction regimens and two postinduction strategies for the treatment of acute nonlymphocytic leukemia: a cancer and leukemia group B study.癌症与白血病B组研究:三种缓解诱导方案及两种诱导后策略治疗急性非淋巴细胞白血病的比较
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Therapy of acute myelogenous leukemia.急性髓性白血病的治疗
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Short-term therapy for acute myelogenous leukemia.急性髓性白血病的短期治疗
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Uncommon subtypes of acute nonlymphocytic leukemia: clinical features and management of FAB M5, M6 and M7.
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Allogeneic and autologous bone marrow transplantation for acute nonlymphocytic leukemia.异基因和自体骨髓移植治疗急性非淋巴细胞白血病。
Semin Oncol. 1987 Dec;14(4):407-15.
10
Current chemotherapeutic treatment approaches to the management of previously untreated adults with de novo acute myelogenous leukemia.目前针对初治成人新发急性髓系白血病的化疗治疗方法。
Semin Oncol. 1987 Dec;14(4):384-96.

高剂量阿糖胞苷联合依托泊苷作为急性髓系白血病的初始治疗:一项单中心研究。

High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study.

作者信息

Parikh P, Powles R, Treleaven J, Helenglass G, Gore M, Rose M, Talbot D, Milan S, Smith C, Pinkerton R

机构信息

Department of Medicine, Royal Marsden Hospital, Sutton, Surrey, UK.

出版信息

Br J Cancer. 1990 Nov;62(5):830-3. doi: 10.1038/bjc.1990.387.

DOI:10.1038/bjc.1990.387
PMID:2245176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1971542/
Abstract

In a single centre, 52 newly diagnosed patients with acute myeloid leukemia (AML) under the age of 56 years received induction chemotherapy commencing with high-dose cytosine arabinoside (Ara-C) and etoposide (Protocol BF11), followed by Ara-C, 6 thioguanine (6TG). A total of 67% of patients entered remission using these drugs. An anthracycline was added for those patients not in remission. The overall remission rate (CR) was 86.5% (45/52), with a minimum follow-up of 90 days. Patients are hospitalised for relatively short periods, and consequently require less blood product and antibiotic support. Patients in continuing first remission following induction with Ara-C and etoposide are similar in number to those in continuing first remission who initially received an anthracycline. This would imply that the efficiency of Ara-C and etoposide in inducing long-term disease-term survival is comparable with anthracycline-containing regimens. We conclude that high-dose Ara-C and etoposide used in the first induction cycle for treating AML have good antileukaemic effect with acceptable toxicity.

摘要

在一个中心,52例年龄在56岁以下新诊断的急性髓系白血病(AML)患者接受了以大剂量阿糖胞苷(Ara-C)和依托泊苷开始的诱导化疗(方案BF11),随后使用阿糖胞苷、6-硫鸟嘌呤(6TG)。使用这些药物,共有67%的患者进入缓解期。对于未缓解的患者加用了蒽环类药物。总缓解率(CR)为86.5%(45/52),最短随访时间为90天。患者住院时间相对较短,因此所需的血液制品和抗生素支持较少。接受阿糖胞苷和依托泊苷诱导后持续首次缓解的患者数量与最初接受蒽环类药物治疗后持续首次缓解的患者数量相似。这意味着阿糖胞苷和依托泊苷诱导长期疾病生存的效率与含蒽环类药物的方案相当。我们得出结论,用于AML首次诱导周期的大剂量阿糖胞苷和依托泊苷具有良好的抗白血病效果,且毒性可接受。